Issue 15, 1993
From the journal:

Journal of the Chemical Society, Chemical Communications

Oxidation of furans with dimethyldioxirane. Interception of malealdehyde and related aldehydes via Wittig reactions

Brian J. Adger,   Collette Barrett,   Joseph Brennan,   Peter McGuigan,   M. Anthony McKervey  and  Brian Tarbit  

Abstract

Unsaturated aldehydes including malealdehyde, generated in acetone by oxidation of furans with dimethyldioxirane, can be trapped efficiently by phosphoranes in Wittig reactions.

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Article information

DOI
https://doi.org/10.1039/C39930001220
Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1220-1222

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Oxidation of furans with dimethyldioxirane. Interception of malealdehyde and related aldehydes via Wittig reactions

B. J. Adger, C. Barrett, J. Brennan, P. McGuigan, M. A. McKervey and B. Tarbit, J. Chem. Soc., Chem. Commun., 1993, 1220 DOI: 10.1039/C39930001220

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